Associated Papers
Identification of a novel nonsense NOG mutation in a patient with stapes ankylosis and symphalangism spectrum disorder.
Sonoyama T et al.
Human Genome Variation, 2023
Identification of an unknown frameshift variant of NOG in a Han Chinese family with proximal symphalangism.
Yuan ZZ et al.
Bioscience Reports, 2020
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.
Ma C et al.
Bmc Medical Genetics, 2019
Identification of a Novel NOG Missense Mutation in a Chinese Family With Symphalangism and Tarsal Coalitions.
Xiong J et al.
Frontiers in Genetics, 2019
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